Evidence map›Paper›PMID 29405930›Full record

ReviewTrends in neurosciences2018

MeCP2 as an Activator of Gene Expression.

Patricia M Horvath, Lisa M Monteggia

Abstract readReview
In one paragraph

Review in Trends in neurosciences, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed.

  1. MECP2Science China. Life sciences · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Diagnostics (Basel, Switzerland) · 2024
    Article
  6. Stroke Causes DNA Methylation atJournal of the American Heart Association · 2024
    Article
  7. Review
  8. Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Article
  14. Role of Virus-Induced Host Cell Epigenetic Changes in Cancer.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Review
  17. Phenotypic features in MECP2 duplication syndrome: Effects of age.American journal of medical genetics. Part A · 2021
    Article
  18. Review
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

2 authors.

Patricia M HorvathDepartment of Neuroscience, The University of Texas Southwestern Medical Center, Dallas, TX 75390-9111, USA.
Lisa M MonteggiaDepartment of Neuroscience, The University of Texas Southwestern Medical Center, Dallas, TX 75390-9111, USA. Electronic address: lisa.monteggia@utsouthwestern.edu.

Funding

ANTIDEPRESSANTS & INTRACELLULAR SIGNALING LINKED TO BDNFR01MH070727 · NIMH · VANDERBILT UNIVERSITY · PI LISA M MONTEGGIA · 2005 to 2026
$8.9M
DIVISION OF CELL &MOLECULAR BIOLOGY TRAINING PROGRAMT32GM008203 · NIGMS · UT SOUTHWESTERN MEDICAL CENTER · PI COBB, MELANIE H. · 1987 to 2018
$7.0M
NIGMS NIH HHS T32 GM008203NIMH NIH HHS R01 MH070727
6 · The paper itself

Abstract

Rett syndrome is a neurodevelopmental disorder that primarily affects females and is caused by mutations in the methyl-CpG-binding-protein 2 (MECP2) gene. Initially, MeCP2 had been shown to be a repressor of gene transcription. In their 2008 paper, Chahrour and colleagues (DOI: 10.1126/science.1153252) reported that MeCP2 could also function as a transcriptional activator.

Indexed as

Genetic Predisposition to DiseaseAnimalsGene ExpressionHumansMethyl-CpG-Binding Protein 2MutationPhenotypeRett SyndromeMethyl-CpG-Binding Protein 2

Identifiers

PMID29405930
PMCPMC5909705

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.